短暂口服抗生素对青春期和成年小鼠内侧前额叶皮层吗啡奖励和基因表达有年龄依赖性影响。

IF 7.6 2区 医学 Q1 IMMUNOLOGY
Rebecca S. Hofford , Jonathon P. Sens , Ava L. Shipman , Violet M. Kimble , Christina Coric , Katherine R. Meckel , Drew D. Kiraly
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引用次数: 0

摘要

青春期是开始有问题的药物使用的关键时期,这大大增加了以后生活中发生物质使用障碍的风险。这种高度的脆弱性部分归因于前额皮质的不成熟,前额皮质是一个对决策和药物奖励都至关重要的大脑区域。在青春期,外围系统,如肠道微生物群,也经历了实质性的变化。新出现的证据表明,肠道微生物群的破坏可以影响啮齿动物模型中的基因表达和药物奖励行为。在这项研究中,我们研究了口服抗生素对吗啡奖励和青春期和成年小鼠前额皮质基因表达的影响。使用口服抗生素暂时破坏微生物组,我们发现短期抗生素暴露降低了吗啡的位置偏好,特别是在青春期小鼠中。在一个单独的队列中,我们观察到抗生素治疗改变了所有年龄组的内侧前额叶皮层对吗啡的转录组反应。值得注意的是,抗生素和吗啡诱导的转录组变化具有年龄特异性,与成人相比,在青少年中观察到不同的基因表达模式。这些发现为未来研究肠道微生物组在阿片类药物奖励中的作用奠定了基础,并强调了阿片类药物敏感性年龄依赖性差异的潜在基因途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Brief exposure to oral antibiotics has age-dependent effects on morphine reward and gene expression in the medial prefrontal cortex of adolescent and adult mice
Adolescence is a critical period for the initiation of problematic drug use, which significantly increases the risk of developing substance use disorders later in life. This heightened vulnerability is partly attributed to the immaturity of the prefrontal cortex, a brain region both essential for decision-making and implicated in drug reward. During adolescence, peripheral systems, such as the gut microbiome, also undergo substantial changes. Emerging evidence suggests that disruptions to the gut microbiome can influence gene expression and drug reward behaviors in rodent models. In this study, we investigated the effects of oral antibiotics on morphine reward and prefrontal cortical gene expression in adolescent and adult mice. Using oral antibiotics to transiently disrupt the microbiome, we found that short-term antibiotic exposure reduced morphine place preference specifically in adolescent mice. In a separate cohort, we observed that antibiotic treatment altered the transcriptomic response to morphine in the medial prefrontal cortex across all age groups. Notably, the transcriptomic changes induced by antibiotics and morphine were age-specific, with distinct gene expression patterns observed in adolescents compared to adults. These findings establish a foundation for future research into the role of the gut microbiome in opioid reward and highlight potential gene pathways underlying age-dependent differences in opioid sensitivity.
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来源期刊
CiteScore
29.60
自引率
2.00%
发文量
290
审稿时长
28 days
期刊介绍: Established in 1987, Brain, Behavior, and Immunity proudly serves as the official journal of the Psychoneuroimmunology Research Society (PNIRS). This pioneering journal is dedicated to publishing peer-reviewed basic, experimental, and clinical studies that explore the intricate interactions among behavioral, neural, endocrine, and immune systems in both humans and animals. As an international and interdisciplinary platform, Brain, Behavior, and Immunity focuses on original research spanning neuroscience, immunology, integrative physiology, behavioral biology, psychiatry, psychology, and clinical medicine. The journal is inclusive of research conducted at various levels, including molecular, cellular, social, and whole organism perspectives. With a commitment to efficiency, the journal facilitates online submission and review, ensuring timely publication of experimental results. Manuscripts typically undergo peer review and are returned to authors within 30 days of submission. It's worth noting that Brain, Behavior, and Immunity, published eight times a year, does not impose submission fees or page charges, fostering an open and accessible platform for scientific discourse.
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